FDA Import Refusal AEK-3641138-4/11/1 — BEIJING GLOBALIPL DEVELOPMENT CO Ltd
The FDA refused shipment AEK-3641138-4/11/1 from BEIJING GLOBALIPL DEVELOPMENT CO Ltd (China) on Jul 26, 2017. The refused product falls under Devices — OVER-THE-COUNTER RADIOFREQUENCY COAGULATION DEVICE FOR WRINKLE REDUCTION. Cited charges: 118,3280 This firm has 4 other import refusals on record.
Refusal details
- Date
- Jul 26, 2017
- Country
- China
- Product Category
- Devices
- Product Code
- 79PAY OVER-THE-COUNTER RADIOFREQUENCY COAGULATION DEVICE FOR WRINKLE REDUCTION
- Charges
- 118,3280